A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204962



Internal ID20772002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28197001..28213500hg38UCSC Ensembl
chr22:28592989..28609488hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3816500
hg1916500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537555
Supporting Variants
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204962
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00054


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